Evidence map›Paper›PMID 22025093›Full record

ArticleCells, tissues, organs2012

Right ventricular outflow tract repair with a cardiac biologic scaffold.

John M Wainwright, Ryotaro Hashizume, Kazuro L Fujimoto, Nathaniel T Remlinger, Colin Pesyna, William R Wagner, Kimimasa Tobita, Thomas W Gilbert, Stephen F Badylak

Abstract read
In one paragraph

Article in Cells, tissues, organs, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed.

  1. AnMaterials today. Communications · 2023
    Article
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  3. Progress in the application of patch materials in cardiovascular surgery.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
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  16. A novel human-derived tissue-engineered patch for vascular reconstruction.American journal of translational research · 2019
    Article
  17. Patch materials for right ventricular outflow reconstruction: past, present, and future.Indian journal of thoracic and cardiovascular surgery · 2019
    Review
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

John M WainwrightDepartment of Surgery, McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pa., USA.
Ryotaro Hashizume
Kazuro L Fujimoto
Nathaniel T Remlinger
Colin Pesyna
William R Wagner
Kimimasa Tobita
Thomas W Gilbert
Stephen F Badylak

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Cardiovascular Bioengineering Training ProgramT32HL076124 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SANJEEV G SHROFF · 2005 to 2026
$7.0M
Cardiac Remodeling with Organ Specific Extracellular Matrix ScaffoldsR03EB009237 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GILBERT, THOMAS W. · 2009 to 2010
$145k
NCATS NIH HHS UL1 TR000005NCRR NIH HHS UL1 RR024153NHLBI NIH HHS T32 HL076124NHLBI NIH HHS T32 HL76124NHLBI NIH HHS T32-HL76124NIBIB NIH HHS 1R03EB009237-01A1NIBIB NIH HHS R03 EB009237NIBIB NIH HHS R03 EB009237-01
6 · The paper itself

Abstract

backgroundSurgical reconstruction of congenital heart defects is often limited by the nonresorbable material used to approximate normal anatomy. In contrast, biologic scaffold materials composed of resorbable non-cross-linked extracellular matrix (ECM) have been used for tissue reconstruction of multiple organs and are replaced by host tissue. Preparation of whole organ ECM by decellularization through vascular perfusion can maintain much of the native three-dimensional (3D) structure, strength, and tissue-specific composition. A 3D cardiac ECM (C-ECM) biologic scaffold material would logically have structural and functional advantages over materials such as Dacron™ for myocardial repair, but the in vivo remodeling characteristics of C-ECM have not been investigated to date. METHODS AND

resultsA porcine C-ECM patch or Dacron patch was used to reconstruct a full-thickness right ventricular outflow tract (RVOT) defect in a rat model with end points of structural remodeling function at 16 weeks. The Dacron patch was encapsulated by dense fibrous tissue and showed little cellular infiltration. Echocardiographic analysis showed that the right ventricle of the hearts patched with Dacron were dilated at 16 weeks compared to presurgery baseline values. The C-ECM patch remodeled into dense, cellular connective tissue with scattered small islands of cardiomyocytes. The hearts patched with C-ECM showed no difference in the size or function of the ventricles as compared to baseline values at both 4 and 16 weeks.

conclusionsThe C-ECM patch was associated with better functional and histomorphological outcomes compared to the Dacron patch in this rat model of RVOT reconstruction.

Indexed as

AnimalsEchocardiographyExtracellular MatrixFemaleHeart Defects, CongenitalHeart VentriclesPolyethylene TerephthalatesRatsRats, Inbred LewSwineTissue EngineeringTissue ScaffoldsPolyethylene Terephthalates

Identifiers

PMID22025093
PMCPMC3325605

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.